Director, Quality Assurance

Avet Pharmaceuticals Inc.; South Brunswick (NJ); On-site; USD 170,000 - 200,000; Full time

Benefits offered by this job

401(k) matching - vested immediately

Medical, Dental, and Vision

Employee Assistance Program

Employee discount through Life Mart

Flexible Spending Account and Dependent Care Account

Job summary

Avet Pharmaceuticals Inc. in South Brunswick, NJ is seeking a Quality Assurance Leader to oversee compliance with cGMP regulations. The ideal candidate will have a Bachelor's degree and at least ten years of experience in QA leadership within a pharmaceutical environment, ensuring successful regulatory inspections and quality standards.

The position offers a salary range of $170,000 to $200,000 per year, eligible for an annual bonus. Benefits include 401(k) matching, medical, dental, and vision coverage.

Qualifications

• Minimum of ten years of progressive Quality Assurance leadership experience.
• Extensive knowledge of current Good Manufacturing Practices (cGMP).
• Demonstrated experience leading regulatory inspections.

Responsibilities

• Provide strategic leadership and oversight of the Quality Assurance department.
• Direct and maintain the organization's quality systems.
• Lead quality oversight of manufacturing operations and suppliers.

Skills

Leadership

Quality Assurance

Regulatory Compliance

Analytical Skills

Communication

Education

Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmacy, or related discipline

Tools

Electronic Quality Management Systems (eQMS)

Microsoft Office Suite

Job description

Reporting Relationships

• This is a supervisory leadership role responsible for overseeing 3 direct reports and 18 indirect reports.

Essential Functions:

• Provide strategic leadership and oversight of the Quality Assurance department to ensure compliance with cGMP regulations, FDA, DEA, and other applicable regulatory requirements.
• Direct and maintain the organization's quality systems to ensure continuous inspection readiness and regulatory compliance across manufacturing operations.
• Serve as the primary site coordinator for regulatory inspections, including FDA, DEA, customer, and third-party audits, ensuring successful inspection outcomes and timely resolution of observations.
• Lead quality oversight of manufacturing operations, contract manufacturers, contract packagers, contract testing laboratories, and suppliers to ensure compliance with established quality standards.
• Develop, implement, and maintain quality compliance strategies, policies, procedures, and systems aligned with business objectives and evolving regulatory requirements.
• Lead and oversee Corrective and Preventive Action (CAPA) activities, ensuring investigations are completed effectively and corrective actions are implemented and sustained.
• Review and approve validation protocols, validation reports, quality system documentation, investigations, deviations, change controls, and other Quality Management System (QMS) records.
• Exercise independent authority for batch disposition decisions, including approval or rejection of manufactured products based on compliance with established quality standards.
• Ensure deviations, nonconformances, and manufacturing investigations are thoroughly evaluated, documented, and resolved in accordance with regulatory expectations.
• Develop, implement, and manage the internal self-inspection program to assess compliance, identify risks, and drive continuous improvement initiatives.
• Oversee vendor qualification and auditing programs, including audits of raw material suppliers, packaging vendors, contract manufacturers, and contract laboratories.
• Partner with cross-functional departments including Research & Development, Manufacturing, Engineering, Technical Services, and Regulatory Affairs to establish compliant processes supporting product development and commercial manufacturing.
• Interface with regulatory agencies and external stakeholders regarding quality-related matters and represent the organization during inspections and compliance activities.
• Facilitate implementation of new quality systems, technologies, and process improvements that enhance compliance and operational efficiency.
• Chair or actively participate in Site Management Review Board (MRB) meetings and provide quality leadership for organizational decision-making.
• Provide leadership, coaching, performance management, and professional development for Quality Assurance personnel while fostering a culture of quality and regulatory compliance.
• Evaluate training needs and ensure personnel maintain required competencies related to cGMP regulations and quality systems.

Specialized Skills and Knowledge:

• Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• Minimum of ten (10) years of progressive Quality Assurance leadership experience within a cGMP-regulated generic pharmaceutical manufacturing environment, including oversight of Oral Solid Dosage (OSD) manufacturing, quality systems, validation, regulatory inspections, and management of Quality Assurance personnel.
• Extensive knowledge of current Good Manufacturing Practices (cGMP), current Good Laboratory Practices (cGLP), FDA regulations, DEA regulations, and applicable domestic and international pharmaceutical regulatory requirements.
• Comprehensive understanding of pharmaceutical manufacturing, quality assurance, quality control, validation, investigations, CAPA, change control, supplier qualification, and audit management.
• Demonstrated experience leading regulatory inspections and managing responses to regulatory observations.
• Strong knowledge of Quality Management Systems (QMS) and risk-based quality management principles.
• Experience interpreting and implementing regulatory guidance, industry standards, and quality compliance requirements.
• Excellent analytical, problem-solving, leadership, organizational, and communication skills.
• Proficiency with electronic Quality Management Systems (eQMS), Microsoft Office Suite, and applicable quality documentation systems.
• Regulatory Compliance & Quality Systems Leadership
• Strategic Leadership & Cross-Functional Collaboration
• Critical Decision-Making, Risk Assessment & Problem Solving

Physical Demands/Factors:

Work is performed in both office and pharmaceutical manufacturing environments. While performing the duties of this position, the employee is regularly required to sit, stand, walk, communicate, and use hands to operate office equipment.

The employee may occasionally be required to reach, bend, stoop, or lift up to 25 pounds. Periodic travel within manufacturing areas and to vendor or contract manufacturing sites may be required. Specific vision abilities include close vision, distance vision, color vision, and the ability to review detailed documentation.

The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions.

Based on the highly regulated workplace at Avet, employees will be required to meet minimum English proficiency requirements.

All applicants must be legally authorized to work in the U.S. for any employer. We are unable to sponsor any applicants for a work visa or take over sponsorship of a work visa for any applicants, at this time.

Avet is proud to be an Equal Opportunity Employer.

This job description is not all-inclusive. It acts as a guideline and is subject to change over time. Additional duties may be assigned based on business needs.

Compensation and Benefits:

Compensation:

This is an exempt salaried position; the pay range is $170,000 to $200,000 per year.

In addition, this position is eligible for an annual bonus which aligns to both individual and company performance.

• 401 (k) matching - vested immediately
• Medical, Dental and Vision
• Employee Assistance Program
• Employee discount through Life Mart
• Flexible Spending Account and Dependent Care Account